1-(Bromomethyl)-3-methoxy-5-nitrobenzene

≥95%

Reagent Code: #150578
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CAS Number 928664-12-4

science Other reagents with same CAS 928664-12-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.06 g/mol
Formula C₈H₈BrNO₃
badge Registry Numbers
MDL Number MFCD18398381
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of nitro-substituted aromatic compounds. Its bromomethyl group allows for easy functionalization through nucleophilic substitution, making it valuable in building complex organic molecules. Commonly employed in the development of dyes and fluorescent probes due to the presence of the nitro and methoxy groups, which influence electronic properties. Also utilized in research settings for the preparation of nitrobenzene derivatives with potential biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,360.00
inventory 250mg
10-20 days ฿11,150.00
inventory 1g
10-20 days ฿23,000.00

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1-(Bromomethyl)-3-methoxy-5-nitrobenzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of nitro-substituted aromatic compounds. Its bromomethyl group allows for easy functionalization through nucleophilic substitution, making it valuable in building complex organic molecules. Commonly employed in the development of dyes and fluorescent probes due to the presence of the nitro and methoxy groups, which influence electronic properties. Also utilized in research settings for the prepa

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of nitro-substituted aromatic compounds. Its bromomethyl group allows for easy functionalization through nucleophilic substitution, making it valuable in building complex organic molecules. Commonly employed in the development of dyes and fluorescent probes due to the presence of the nitro and methoxy groups, which influence electronic properties. Also utilized in research settings for the preparation of nitrobenzene derivatives with potential biological activity.

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